Hydroboration of Allenes

D Devaprabhakara, PD Gardner

Index: Devaprabhakara,D.; Gardner,P.D. Journal of the American Chemical Society, 1963 , vol. 85, p. 1458 - 1460

Full Text: HTML

Citation Number: 20

Abstract

(1 9.59). afforded mainly cyclononanone. A smaller amount of cyclononanol and cis- cyclononene was also obtained. These results suggest that the principal organoborane, tris- 1-cyclononenylborane, is that formed from attack of boron at the central carbon atom of the allene linkage. It is the organoborane which would be formed by hydroboration of cyclononyne.'The formation of cyclononene is best interpreted as evidence for the ...

Related Articles:

β'β Anionic elimination of carboxylic esters

[Aubert, Corinne; Begue, Jean-Pierre; Biellmann, Jean-Francois Tetrahedron, 1986 , vol. 42, # 20 p. 5581 - 5590]

Alicyclic reaction mechanisms. 7. The predominance and quantification of steric effects in the solvolysis of secondary aliphatic esters

[Schneider, Hans-Joerg; Becker, Norman; Schmidt, Guenther; Thomas, Fred Journal of Organic Chemistry, 1986 , vol. 51, # 19 p. 3602 - 3607]

Vitamine, provitamine und carotinoide

[Prelog et al. Helvetica Chimica Acta, 1953 , vol. 36, p. 471,479]

More Articles...